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How Compounded Medications Are Regulated Compounding pharmacies must follow rules set by: State boards of pharmacy (licensing, inspections, complaint handling) USP (United States Pharmacopeia) standards for sterile and non-sterile compounding FDA oversight for 503B facilities and certain higher-risk activities High-quality pharmacies typically: Use high-quality API from FDA-registered or reputable international manufacturers Test for potency (does the medication contain the amount of drug it says?) Test for sterility and endotoxins for injectable medications Use cleanroom environments and specialized hoods for sterile compounding Track lots and beyond-use dates (expiration) to support stability and traceability Where Things Can Go Wrong Risks increase when pharmacies: Use the wrong form of the drug (for example, semaglutide sodium instead of semaglutide base) Cut corners on sterility testing or cleanroom standards Do not verify potency or rely on unvetted suppliers Sell products without real prescriptions or market them as research chemicals The FDA has specifically warned about: Compounded semaglutide products using salt forms (semaglutide sodium, semaglutide acetate) that are not the same as the approved drug and have not been proven safe or effective for weight loss in humans

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Gene lists of complete first and second level networks are provided in Supplementary data 1 in spreadsheet networks_genes

This process breaks down the cells into smaller parts

2002;12:S215